A framework for the investigation of rare genetic disorders in neuropsychiatry
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DOI: 10.1038/s41591-019-0581-5
Abstract: De novo and inherited rare genetic disorders (RGDs) are a major cause of human morbidity, frequently involving neuropsychiatric symptoms. Recent advances in genomic technologies and data sharing have revolutionized the identification and diagnosis of RGDs,… read more here.
Keywords: investigation rare; disorders neuropsychiatry; genetic disorders; framework investigation ... See more keywords